| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 164851 | BAA02g11170 | A02 | 5052746 | G | A | missense_variant | MODERATE | c.425C>T|p.Thr142Ile |
S74 |
| 164852 | BAA02g11170 | A02 | 5052998 | C | T | stop_gained | HIGH | c.173G>A|p.Trp58* |
S172 S217 |
| 164853 | BAA02g11170 | A02 | 5053408 | G | A | upstream_gene_variant | MODIFIER | c.-238C>T| |
S158 |
| 164854 | BAA02g11170 | A02 | 5054153 | C | T | upstream_gene_variant | MODIFIER | c.-983G>A| |
S272 |
| 164855 | BAA02g11170 | A02 | 5054599 | G | A | upstream_gene_variant | MODIFIER | c.-1429C>T| |
S210 S225 |
| 164856 | BAA02g11170 | A02 | 5055587 | C | T | upstream_gene_variant | MODIFIER | c.-2417G>A| |
S257 |
| 164857 | BAA02g11180 | A02 | 5058307 | G | A | missense_variant | MODERATE | c.160G>A|p.Glu54Lys |
S143 |
| 164858 | BAA02g11180 | A02 | 5058819 | G | A | downstream_gene_variant | MODIFIER | c.*372G>A| |
S19 |
| 164859 | BAA02g11190 | A02 | 5059666 | C | T | missense_variant | MODERATE | c.733G>A|p.Gly245Ser |
S178 |
| 164860 | BAA02g11190 | A02 | 5059790 | C | T | synonymous_variant | LOW | c.609G>A|p.Glu203Glu |
S255 |
| 164861 | BAA02g11190 | A02 | 5059920 | G | A | missense_variant | MODERATE | c.479C>T|p.Pro160Leu |
S136 |
| 164862 | BAA02g11190 | A02 | 5060175 | G | A | missense_variant | MODERATE | c.311C>T|p.Thr104Ile |
S289 S290 |
| 164863 | BAA02g11190 | A02 | 5060521 | G | A | upstream_gene_variant | MODIFIER | c.-36C>T| |
S125 |
| 164864 | BAA02g11200 | A02 | 5062181 | C | T | missense_variant | MODERATE | c.910G>A|p.Ala304Thr |
S123 |
| 164865 | BAA02g11200 | A02 | 5062208 | C | T | missense_variant | MODERATE | c.883G>A|p.Asp295Asn |
S81 S85 |
| 164866 | BAA02g11200 | A02 | 5063258 | G | A | missense_variant | MODERATE | c.223C>T|p.Arg75Cys |
S61 |
| 164867 | BAA02g11190 | A02 | 5064319 | G | A | upstream_gene_variant | MODIFIER | c.-3834C>T| |
S276 |
| 164868 | BAA02g11210 | A02 | 5064376 | G | A | missense_variant | MODERATE | c.1076C>T|p.Ala359Val |
S125 |
| 164869 | BAA02g11210 | A02 | 5064653 | G | A | synonymous_variant | LOW | c.918C>T|p.His306His |
S111 |
| 164870 | BAA02g11210 | A02 | 5065335 | C | T | missense_variant | MODERATE | c.481G>A|p.Gly161Arg |
S179 |
| 164871 | BAA02g11190 | A02 | 5065395 | G | A | upstream_gene_variant | MODIFIER | c.-4910C>T| |
S288 |
| 164872 | BAA02g11210 | A02 | 5065546 | C | T | synonymous_variant | LOW | c.375G>A|p.Gln125Gln |
S226 |
| 164873 | BAA02g11210 | A02 | 5065578 | C | T | missense_variant | MODERATE | c.343G>A|p.Glu115Lys |
S1 S90 |
| 164874 | BAA02g11200 | A02 | 5066624 | C | T | upstream_gene_variant | MODIFIER | c.-3144G>A| |
S167 |
| 164875 | BAA02g11200 | A02 | 5066757 | C | T | upstream_gene_variant | MODIFIER | c.-3277G>A| |
S292 |